EP0358265B1 - Catalyst component and catalyst for the polymerization of ethylene and the copolymerization of ethylene with alpha-olefins - Google Patents

Catalyst component and catalyst for the polymerization of ethylene and the copolymerization of ethylene with alpha-olefins Download PDF

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Publication number
EP0358265B1
EP0358265B1 EP89202199A EP89202199A EP0358265B1 EP 0358265 B1 EP0358265 B1 EP 0358265B1 EP 89202199 A EP89202199 A EP 89202199A EP 89202199 A EP89202199 A EP 89202199A EP 0358265 B1 EP0358265 B1 EP 0358265B1
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EP
European Patent Office
Prior art keywords
ethylene
arene
catalyst component
aluminium
temperature
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
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EP89202199A
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German (de)
English (en)
French (fr)
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EP0358265A3 (en
EP0358265A2 (en
Inventor
Fausto Calderazzo
Guido Pampaloni
Francesco Masi
Angelo Moalli
Renzo Invernizzi
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Versalis SpA
Original Assignee
Enichem SpA
Enichem Anic SpA
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Priority to AT89202199T priority Critical patent/ATE97671T1/de
Publication of EP0358265A2 publication Critical patent/EP0358265A2/en
Publication of EP0358265A3 publication Critical patent/EP0358265A3/en
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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/26Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
    • B01J31/38Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24 of titanium, zirconium or hafnium
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F10/00Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F10/02Ethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F10/00Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond

Definitions

  • This invention relates to a solid catalyst component and a catalyst for the polymerization of ethylene and the copolymerization of ethylene with C3-C10 alpha-olefins.
  • the invention also relates to the use of said catalyst component and said catalyst in low pressure, low temperature suspension polymerization processes, in high pressure, high temperature processes conducted in a tubular reactor or pressure vessel, and in high temperature processes conducted in solution.
  • catalysts are used generally formed from a compound of group IV to group VI elements of the periodic table (transition metal compounds), mixed with an organometallic compound or hydride of group I to group III elements of the periodic table, operating in solution, in suspension or in the gaseous phase.
  • transition metal compounds transition metal compounds
  • organometallic compound or hydride of group I to group III elements of the periodic table operating in solution, in suspension or in the gaseous phase.
  • Catalysts are also known in which the transition metal is fixed to a solid organic or inorganic support which has possibly been physically and/or chemically treated.
  • the transition metal generally used for this purpose is titanium, which results in high yields and high productivity, especially in ethylene polymerization.
  • Use is also made of combinations of titanium with other transition metals such as vanadium, zirconium or hafnium in the preparation of ethylene polymers or copolymers with specific characteristics.
  • the titanium-vanadium combination is often used in the preparation of ethylene copolymers with homogeneous distribution of the comonomer in the macromolecule, which have good mechanical characteristics and improved workability.
  • These catalyst components are generally obtained by bringing a titanium compound (generally titanium tetrachloride), a vanadium compound (generally vanadium oxychloride) and an alkyl aluminium chloride into contact under reaction conditions, as described for example in European patent application, publication No. 57,050.
  • the main drawback of these catalyst components is their relatively low polymerization activity, with the result that costly purification of the polymer from the catalytic residues is required.
  • a further drawback is the difficulty of reproducibly preparing catalysts having the desired characteristics. It is also known from U.S. patents 4,037,041 and 4,151,110 to prepare catalyst components from titanium tetrachloride and vanadium carbonyl as zerovalent vanadium compound. However even these catalyst components demonstrate poor activity under normal polymerization conditions, and in addition vanadium carbonyls are compounds which are difficult to produce and handle, making them unsuitable for use in a commercial plant.
  • a new catalyst component containing titanium and vanadium has now been found which is stable and highly active in ethylene (co)polymerization conducted at low or high pressure or in solution, and is able to produce ethylene (co)polymers having good mechanical and workability characteristics.
  • Examples of arenes are: benzene, toluene, p-xylene and mesitylene. Of these, benzene is preferred.
  • Vanadium arenes are compounds known in the art and can be prepared as described for example by E.O. Fisher and H.S. Kogler in Chem. Ber. 90, 250 (1957), and by F. Calderazzo in Inorg. Chem. 3, 810 (1964).
  • the vanadium arene is dissolved in an inert liquid organic solvent, preferably an aliphatic hydrocarbon such as heptane, octane, nonane and decane, titanium tetrachloride then being added to the obtained solution in a quantity such that the Ti/V atomic ratio is within the range of 1/1 to 3/1 and preferably of the order of 2/1.
  • an inert liquid organic solvent preferably an aliphatic hydrocarbon such as heptane, octane, nonane and decane
  • the procedure is carried out at a temperature of between 20 and 120°C, and preferably of the order of 90-100°C, for a time of between a few seconds (for example 5-10 seconds) and 24 hours, with precipitation of the solid catalyst component.
  • the short contact times are useful in the case of in-line feed to the polymerization reactor, in which the solid component precursors, in solution form in an organic solvent, are mixed together immediately before being fed to the reactor.
  • the solid catalyst component is produced and used directly in line in the form of a suspension in its mother liquor.
  • the precipitated solid catalyst component is separated from the suspension by the usual methods such as filtration, decantation or centrifuging, and is washed with an inert liquid organic solvent, especially a hydrocarbon solvent such as heptane, operating at a temperature between ambient and the boiling point of the solvent used.
  • the catalyst component obtained in this manner is a solid amorphous to X-rays, and in the form of particles of size between 5 and 20 ⁇ m, of apparent density between 0.2 and 0.35 g/ml, of surface area between 20 and 70 m2/g and of pore radius between 10,000 and 20,000 ⁇ .
  • the solid catalyst component prepared as described heretofore is treated with an alkyl aluminium chloride and preferably with diethyl aluminium monochloride, monoethyl aluminium dichloride or ethyl aluminium sesquichoride.
  • This procedure is conveniently carried out with the solid catalyst component suspended in an inert liquid organic solvent, preferably an aliphatic hydrocarbon such as heptane, octane, nonane or decane, at a temperature of between 20 and 80°C for a time depending on the chosen temperature and generally between 0.3 and 3 hours, and with an atomic ratio of aluminium in the alkyl aluminium chloride to titanium in the solid temperature component of between 1/1 and 5/1.
  • an inert liquid organic solvent preferably an aliphatic hydrocarbon such as heptane, octane, nonane or decane
  • the preferred operating conditions are an atomic Al/Ti ratio of the order of 1/1-1.5/1, ambient temperature and a time of about one hour.
  • the solid catalyst component treated in this manner is conveniently washed with an inert liquid organic solvent, especially an aliphatic hydrocarbon, operating under the aforesaid conditions. This treatment generally results in an increase in surface area and a reduction in average particle diameter and mean pore radius, these values however still falling within the aforesaid ranges, and produces a solid catalyst component generally having higher activity than the non-treated component.
  • the catalyst according to the present invention is formed from the described solid component plus a trialkyl aluminium containing from 2 to 8 and preferably from 2 to 4 carbon atoms in the alkyl portion. Triethyl aluminium and triisobutyl aluminium are preferred.
  • the atomic ratio of the aluminium (in the trialkyl aluminium) to the sum of the titanium and vanadium (in the solid catalyst component) varies from 2/1 to 50/1, the upper limit of said ratio not being critical but being dictated mainly by economic reasons.
  • this ratio vary from 3/1 to 7/1, such values giving improved polymer yields.
  • low ratios are advantageous in high temperature polymerization because they prevent the trialkyl aluminium becoming involved in reduction reactions with the production of species which are inactive for polymerization purposes.
  • the catalyst of the present invention is active in the polymerization of ethylene and the copolymerization of ethylene with C3-C10 alpha-olefins.
  • the catalyst is active within a wide range of conditions, and most particularly in the low temperature, low pressure processes normally used in the suspension method, in the high temperature, high pressure processes conducted in tubular reactions or pressure vessels, and in the high temperature processes conducted in solution.
  • Processes in suspension are conducted generally in the presence of a diluent, at a temperature of between 60 and 100°C and a pressure of between 5 and 15 atg, in the presence of hydrogen as moderator.
  • High temperature, high pressure processes are conducted generally at a temperature of between 100 and 280°C at a pressure of between 800 and 1800 atg.
  • Processes in solution are conducted generally at a temperature of the order of 150-300°C.
  • the catalysts of the present invention enable polymers to be obtained which have a molecular weight distribution ranging from medium to wide, and are particularly suitable for transformation by methods such as blow moulding in the manufacture of film and miscellaneous articles, and injection moulding.
  • the catalysts of the present invention enable low-density linear polymers to be obtained which are particularly suitable for transformation by blow moulding or injection moulding, depending on the molecular weight distribution.
  • the catalysts of the present invention demonstrate a polymerization activity which is unexpectedly high considering the titanium and vanadium-based catalysts of the known art.
  • (benzene)2
  • E.O. Fisher H.S. Kogler and F. Calderazzo
  • the catalyst component contains 22.9% titanium, 13.0% vanadium and 64.1% chlorine w/w.
  • the catalyst component can be represented by the formula: Ti (1.9), V (1), Cl (7.2).
  • the catalyst component contains 22.7% titanium, 11.5% vanadium and 65.8% chlorine w/w.
  • the catalyst component can be represented by the formula: Ti (2.1), V (1), Cl (8.4).
  • 0.3 g of solid catalyst component are obtained having the following characteristics: titanium content: 21.4% by weight, expressed as metal, specific surface area: 55 m2/g, apparent density: 0.22 g/ml, mean pore radius: 8,000 ⁇ , average particle diameter: 8 ⁇ m.
  • the catalyst component contains 21.4% titanium, 12.0% vanadium and 66.6% chlorine w/w.
  • the catalyst component can be represented by the formula: Ti (1.9), V (1), Cl (8).
  • Example 3 0.3 g of solid catalyst component are obtained having the following characteristics: titanium content: 21.9% by weight, expressed as metal, specific surface area: 70 m2/g, apparent density: 0.19 g/ml, mean pore radius: 5,000 ⁇ , average particle diameter: 6 ⁇ m.
  • the catalyst component contains 21.9% titanium, 11.6% vanadium and 66.4% chlorine w/w.
  • the catalyst component can be represented by the formula: Ti (2.0), V (1), Cl (8.2).
  • solid catalyst component having the following characteristics: titanium content: 24.8% by weight, expressed as metal, specific surface area: 32 m2/g, apparent density: 0.26 g/ml, mean pore radius: 13,000 ⁇ , average particle diameter: 11 ⁇ m.
  • the catalyst component contains 24.8% titanium, 8.5% vanadium and 66.7% chlorine w/w.
  • the catalyst component can be represented by the formula: Ti (3.1), V (1), Cl (11.3).
  • 0.7 g of solid catalyst component are obtained having the following characteristics: titanium content: 17.9% by weight, expressed as metal, specific surface area: 20 m2/g, apparent density: 0.32 g/ml, mean pore radius: 18,000 ⁇ , average particle diameter: 14 ⁇ m.
  • the catalyst component contains 17.9% titanium, 9.5% vanadium and 72.6% chlorine w/w.
  • the catalyst component can be represented by the formula: Ti (2), V (1), Cl (11).
  • solid catalyst component having the following characteristics: titanium content: 5.8% by weight, expressed as metal, specific surface area: 36 m2/g, apparent density: 0.28 g/ml, mean pore radius: 14,000 ⁇ , average particle diameter: 14 ⁇ m.
  • the catalyst component contains 5.8% titanium, 23.9% vanadium and 70.3% chlorine w/w.
  • the catalyst component can be represented by the formula: Ti (1), V (3.9), Cl (16.5).
  • a polyethylene is recovered in accordance with the following values: productivity: 9.2 kg, expressed as kg of polyethylene per gram of solid catalyst component, yield: 40 kg, expressed as kg of polyethylene per gram of titanium in the solid catalyst component, yield: 75.5 kg, expressed as kg of polyethylene per gram of vanadium in the solid catalyst component.
  • the polyethylene produced in this manner has the following characteristics: Melt index: 0.28 g/10 min (ASTM-D 1238 F), Shear sensitivity: 12.8 (ASTM-D 1238 F), Density: 0.955 g/ml (ASTM-D 2839), Apparent density: 0.18 g/ml.
  • the polyethylene obtained has the following characteristics: Melt index: 0.25 g/10 min, Shear sensitivity: 13.0, Density: 0.955 g/ml, Apparent density: 0.20 g/ml.
  • the copolymer produced in this manner has the following characteristics: Melt index: 0.34 g/10 min, Shear sensitivity: 12.4, Density: 0.940 g/ml, Apparent density: 0.15 g/ml.
  • the copolymer produced in this manner has the following characteristics: Melt index: 0.32 g/10 min, Shear sensitivity: 12.5, Density: 0.942 g/ml, Apparent density: 0.16 g/ml.
  • the polyethylene produced in this manner has the following characteristics: Melt index: 0.32 g/10 min, Shear sensitivity: 12.8, Density: 0.956 g/ml, Apparent density: 0.22 g/ml.
  • the polyethylene produced in this manner has the following characteristics: Melt index: 0.22 g/10 min, Shear sensitivity: 13.4, Density: 0.954 g/ml, Apparent density: 0.22 g/ml.
  • the polyethylene produced in this manner has the following characteristics: Melt index: 0.32 g/10 min, Shear sensitivity: 12.8, Density: 0.956 g/ml, Apparent density: 0.24 g/ml.
  • a steel reactor vessel with a volume of 1.5 litres fitted with a stirrer and heat transfer jacket for controlling the reaction temperature is used.
  • a 20 kg/hour throughput of a mixture (50:50 w/w of ethylene and 1-butene is fed into one end of the reactor by a reciprocating compressor.
  • 80 ml/hour of a suspension in the form of a C10-C12 isoparaffin mixture containing 1.7 g/litre of the solid catalyst component prepared as described in Example 4 is fed into the same end of the reactor by an intensifier pump.
  • Triethyl aluminium in the form of a 10% w/w solution in a C10-C12 isoparaffin mixture is also fed into the end of the reactor by an intensifier pump in a quantity of 180 ml/hour so that the atomic ratio of the aluminium in said triethyl aluminium to the titanium is said solid catalyst component is 15/1.
  • Polymerization is conducted under the following conditions: reactor inlet pressure: 1200 atg, reactor inlet temperature: 60°C, polymerization temperature: 270°C, residence time in reactor: 2 minutes.
  • the reaction is conducted continuously, 10 ml/hour of glycerin being added to the reactor outlet stream to activate the catalyst.
  • the conversion calculated on the ethylene is 17.5%, the polymer being recovered by using a multistage flash chamber, the polymer being fed directly from said flash chamber to the extruder.
  • the unaltered monomers are recycled to the reactor inlet after being purified and made up with fresh monomers.
  • productivity 25.2 kg
  • yield with respect to the vanadium
  • yield with respect to the titanium
  • the copolymer has the following characteristics: Melt index: 1.1 g/10 min, Shear sensitivity: 37, Density: 0.9290 g/ml.
  • Example 15 The procedure of Example 15 is followed, but using the solid catalyst component of Example 7.
  • An ethylene/1-butene copolymer is obtained with the following values: productivity: 11.6 kg, yield (with respect to the vanadium): 48.3 kg, yield (with respect to the titanium): 200 kg,
  • the copolymer has the following characteristics: Melt index: 1.0 g/10 min, Shear sensitivity: 39, Density: 0.9290 g/ml.
  • the reactor temperature is raised to 90°C and the reactor is then pressurized with hydrogen to 2.0 atg and then with ethylene to 6.5 atg.
  • the procedure of Example 8 is followed polymerizing for 1 hour, to obtain a polyethylene with: productivity: 4.2 kg, yield (with respect to the titanium): 23.5 kg, yield (with respect to the vanadium): 44 kg.
  • the polyethylene produced in this manner has the following characteristics: Melt index: 0.44 g/10 min, Shear sensitivity: 12.0, Density: 0.955 g/ml, Apparent density: 0.27 g/ml.
  • the polyethylene produced in this manner has the following characteristics: Melt index: 0.24 g/10 min, Shear sensitivity: 12.0, Density: 0.956 g/ml, Apparent density: 0.18 g/ml.
  • the polyethylene produced in this manner has the following characteristics: Melt index: 0.4 g/10 min, Shear sensitivity: 48, Density: 0.959 g/ml, Apparent density: 0.20 g/ml.
  • the polyethylene produced in this manner has the following characteristics: Melt index: 0.35 g/10 min, Shear sensitivity: 48, Density: 0.958 g/ml, Apparent density: 0.2 g/ml.
  • the polyethylene produced in this manner has the following characteristics: Melt index: 0.21 g/10 min, Shear sensitivity: 13, Density: 0.955 g/ml, Apparent density: 0.17 g/ml.
  • Polymerization is interrupted as in the preceding examples, to recover a polyethylene with: productivity: 7 kg, yield (with respect to the vanadium): 58.6 kg. yield (with respect to the titanium): 31.2 kg,
  • productivity 7 kg
  • yield with respect to the vanadium
  • yield with respect to the titanium
  • yield with respect to the titanium
  • the polyethylene produced in this manner has the following characteristics: Melt index: 0.23 g/10 min, Shear sensitivity: 13, Density: 0.955 g/ml, Apparent density: 0.22 g/ml.
  • the process is continued for 1 hour, to recover a polyethylene with: productivity: 31.6 kg, yield (with respect to the vanadium): 264 kg. yield (with respect to the titanium): 141 kg,
  • the polyethylene produced in this manner has the following characteristics: Melt index: 0.24 g/10 min, Shear sensitivity: 46, Density: 0.9585 g/ml, Apparent density: 0.20 g/ml.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
EP89202199A 1988-09-09 1989-08-31 Catalyst component and catalyst for the polymerization of ethylene and the copolymerization of ethylene with alpha-olefins Expired - Lifetime EP0358265B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT89202199T ATE97671T1 (de) 1988-09-09 1989-08-31 Katalysatorbestandteil und katalysator zur polymerisation von ethylen oder copolymerisation von ethylen mit alpha-olefinen.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IT8821876A IT1227053B (it) 1988-09-09 1988-09-09 Componente di catalizzatore e gatalizzatore per la polimerizzazione di etilene e per la copolimerizzazione di etilene con alfa olefine.
IT2187688 1988-09-09

Publications (3)

Publication Number Publication Date
EP0358265A2 EP0358265A2 (en) 1990-03-14
EP0358265A3 EP0358265A3 (en) 1991-06-12
EP0358265B1 true EP0358265B1 (en) 1993-11-24

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EP89202199A Expired - Lifetime EP0358265B1 (en) 1988-09-09 1989-08-31 Catalyst component and catalyst for the polymerization of ethylene and the copolymerization of ethylene with alpha-olefins

Country Status (15)

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US (1) US4987111A (zh)
EP (1) EP0358265B1 (zh)
JP (1) JP2759350B2 (zh)
KR (1) KR920006446B1 (zh)
CN (1) CN1034811C (zh)
AT (1) ATE97671T1 (zh)
BR (1) BR8904621A (zh)
CA (1) CA1335093C (zh)
DE (1) DE68910908T2 (zh)
EG (1) EG18937A (zh)
ES (1) ES2059706T3 (zh)
FI (1) FI96614C (zh)
IT (1) IT1227053B (zh)
NO (1) NO171918C (zh)
ZA (1) ZA896770B (zh)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU647296B2 (en) * 1991-07-12 1994-03-17 Ecp Enichem Polimeri S.R.L. Procedure for the producing of vanadium bis-arenes from vanadium oxychloride
IT1263862B (it) * 1993-03-31 1996-09-04 Enichem Polimeri Procedimento per la (co)polimerizzazione dell'etilene
IT1269805B (it) * 1994-05-20 1997-04-15 Enichem Spa Catalizzatore per la (co)polimerizzazione dell'etilene e procedimento per il suo ottenimento
IT1284927B1 (it) * 1996-10-08 1998-05-28 Enichem Elastomers Procedimento per la preparazione di copolimeri etilene propilene a basso tenore in cloro residuo
IT1403290B1 (it) 2010-12-27 2013-10-17 Polimeri Europa Spa Componente solido di catalizzatore, catalizzatore comprendente detto componente solido, e procedimento di (co)polimerizzazione delle alfa-olefine

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3378536A (en) * 1964-09-24 1968-04-16 Phillips Petroleum Co Polymerization process using a catalyst comprising a supported diarene metal and supported chromium oxide
US4111834A (en) * 1975-05-28 1978-09-05 Imperial Chemical Industries Limited Process for preparing a transition metal compound and it's use as a component in an olefin polymerization catalyst
US4267293A (en) * 1978-05-19 1981-05-12 Phillips Petroleum Company Method for producing ethylene polymers using treated catalysts containing titanium and vanadium
US4325839A (en) * 1979-12-21 1982-04-20 Phillips Petroleum Company Impregnated second valence chromium compound in supported catalyst
CA1171065A (en) * 1981-01-06 1984-07-17 Vaclav G. Zboril Process for the preparation of polymers of alpha- olefins at high temperatures
US4525551A (en) * 1982-03-12 1985-06-25 Eastman Kodak Company Highly active and efficient polyolefin catalyst

Also Published As

Publication number Publication date
FI96614B (fi) 1996-04-15
ATE97671T1 (de) 1993-12-15
JP2759350B2 (ja) 1998-05-28
ZA896770B (en) 1990-06-27
NO171918B (no) 1993-02-08
CN1040989A (zh) 1990-04-04
NO893576D0 (no) 1989-09-06
DE68910908T2 (de) 1994-05-05
CA1335093C (en) 1995-04-04
JPH02107604A (ja) 1990-04-19
US4987111A (en) 1991-01-22
EP0358265A3 (en) 1991-06-12
FI894236A (fi) 1990-03-10
NO893576L (no) 1990-03-12
EP0358265A2 (en) 1990-03-14
IT1227053B (it) 1991-03-14
NO171918C (no) 1993-05-19
IT8821876A0 (it) 1988-09-09
FI96614C (fi) 1996-07-25
ES2059706T3 (es) 1994-11-16
KR900004403A (ko) 1990-04-12
CN1034811C (zh) 1997-05-07
FI894236A0 (fi) 1989-09-08
KR920006446B1 (ko) 1992-08-06
EG18937A (en) 1994-03-30
BR8904621A (pt) 1990-04-24
DE68910908D1 (de) 1994-01-05

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